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EMA approval · 2023-06-01

EMA Authorised: Rapilysin (reteplase) — Actavis Group PTC ehf

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Summary

Rapilysin (reteplase) has been authorised in the EU for myocardial infarction, with Actavis Group PTC ehf as the marketing authorisation holder.

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Diseases / indications

Drugs mentioned

  • Rapilysin (reteplase)

Snippet

Status: Authorised. Therapeutic area: Myocardial Infarction. MAH: Actavis Group PTC ehf. Decision date: 31/05/2023